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Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma

The use of circulating microRNAs as biomarkers has opened new opportunities for diagnosis of cancer because microRNAs exhibit tumor-specific expression profiles. The aim of this study was the identification of circulating microRNAs in human plasma as potential biomarkers for the diagnosis of maligna...

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Autores principales: Weber, Daniel G., Gawrych, Katarzyna, Casjens, Swaantje, Brik, Alexander, Lehnert, Martin, Taeger, Dirk, Pesch, Beate, Kollmeier, Jens, Bauer, Torsten T., Johnen, Georg, Brüning, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339541/
https://www.ncbi.nlm.nih.gov/pubmed/28321148
http://dx.doi.org/10.1155/2017/9280170
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author Weber, Daniel G.
Gawrych, Katarzyna
Casjens, Swaantje
Brik, Alexander
Lehnert, Martin
Taeger, Dirk
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Johnen, Georg
Brüning, Thomas
author_facet Weber, Daniel G.
Gawrych, Katarzyna
Casjens, Swaantje
Brik, Alexander
Lehnert, Martin
Taeger, Dirk
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Johnen, Georg
Brüning, Thomas
author_sort Weber, Daniel G.
collection PubMed
description The use of circulating microRNAs as biomarkers has opened new opportunities for diagnosis of cancer because microRNAs exhibit tumor-specific expression profiles. The aim of this study was the identification of circulating microRNAs in human plasma as potential biomarkers for the diagnosis of malignant mesothelioma. For discovery, TaqMan Low Density Array Human MicroRNA Cards were used to analyze 377 microRNAs in plasma samples from 21 mesothelioma patients and 21 asbestos-exposed controls. For verification, individual TaqMan microRNA assays were used for quantitative real-time PCR in plasma samples from 22 mesothelioma patients and 44 asbestos-exposed controls. The circulating miR-132-3p showed different expression levels between mesothelioma patients and asbestos-exposed controls. For discrimination, sensitivity of 86% and specificity of 61% were calculated. Circulating miR-132-3p in plasma was not affected by hemolysis and no impact of age or smoking status on miR-132-3p levels could be observed. For the combination of miR-132-3p with the previously described miR-126, sensitivity of 77% and specificity of 86% were calculated. The results of this study indicate that miR-132-3p might be a new promising diagnostic biomarker for malignant mesothelioma. It is indicated that the combination of miR-132-3p with other individual biomarkers improves the biomarker performance.
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spelling pubmed-53395412017-03-20 Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma Weber, Daniel G. Gawrych, Katarzyna Casjens, Swaantje Brik, Alexander Lehnert, Martin Taeger, Dirk Pesch, Beate Kollmeier, Jens Bauer, Torsten T. Johnen, Georg Brüning, Thomas Dis Markers Research Article The use of circulating microRNAs as biomarkers has opened new opportunities for diagnosis of cancer because microRNAs exhibit tumor-specific expression profiles. The aim of this study was the identification of circulating microRNAs in human plasma as potential biomarkers for the diagnosis of malignant mesothelioma. For discovery, TaqMan Low Density Array Human MicroRNA Cards were used to analyze 377 microRNAs in plasma samples from 21 mesothelioma patients and 21 asbestos-exposed controls. For verification, individual TaqMan microRNA assays were used for quantitative real-time PCR in plasma samples from 22 mesothelioma patients and 44 asbestos-exposed controls. The circulating miR-132-3p showed different expression levels between mesothelioma patients and asbestos-exposed controls. For discrimination, sensitivity of 86% and specificity of 61% were calculated. Circulating miR-132-3p in plasma was not affected by hemolysis and no impact of age or smoking status on miR-132-3p levels could be observed. For the combination of miR-132-3p with the previously described miR-126, sensitivity of 77% and specificity of 86% were calculated. The results of this study indicate that miR-132-3p might be a new promising diagnostic biomarker for malignant mesothelioma. It is indicated that the combination of miR-132-3p with other individual biomarkers improves the biomarker performance. Hindawi Publishing Corporation 2017 2017-02-21 /pmc/articles/PMC5339541/ /pubmed/28321148 http://dx.doi.org/10.1155/2017/9280170 Text en Copyright © 2017 Daniel G. Weber et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Weber, Daniel G.
Gawrych, Katarzyna
Casjens, Swaantje
Brik, Alexander
Lehnert, Martin
Taeger, Dirk
Pesch, Beate
Kollmeier, Jens
Bauer, Torsten T.
Johnen, Georg
Brüning, Thomas
Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title_full Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title_fullStr Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title_full_unstemmed Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title_short Circulating miR-132-3p as a Candidate Diagnostic Biomarker for Malignant Mesothelioma
title_sort circulating mir-132-3p as a candidate diagnostic biomarker for malignant mesothelioma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339541/
https://www.ncbi.nlm.nih.gov/pubmed/28321148
http://dx.doi.org/10.1155/2017/9280170
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